ChemicalBook > CAS DataBase List > 2-METHOXY-1,4-NAPHTHOQUINONE

2-METHOXY-1,4-NAPHTHOQUINONE

Product Name
2-METHOXY-1,4-NAPHTHOQUINONE
CAS No.
2348-82-5
Chemical Name
2-METHOXY-1,4-NAPHTHOQUINONE
Synonyms
Lawsone methyl ether;2-Methoxynaphthoquinone;2-methoxy-4-naphthoquinone;2-Methoxy-p-naphthoquinone;2-Methoxy-1,4-naphtoquinone;2-METHOXY-1,4-NAPHTHOQUINONE;2-methoxy-4-naphthalenedione;2-methoxynaphthalene-1,4-dione;2-methoxy-1,4-naphthalenedione;1,4-Naphthoquinone, 2-methoxy-
CBNumber
CB0287319
Molecular Formula
C11H8O3
Formula Weight
188.18
MOL File
2348-82-5.mol
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2-METHOXY-1,4-NAPHTHOQUINONE Property

Melting point:
184-187 °C(lit.)
Boiling point:
283.17°C (rough estimate)
Density 
1.2100 (rough estimate)
refractive index 
1.6400 (estimate)
storage temp. 
Store at -20°C
solubility 
DMSO : 50 mg/mL (265.70 mM; Need ultrasonic)
form 
Solid
color 
Light yellow to yellow
Water Solubility 
31.23mg/L(temperature not stated)
EPA Substance Registry System
2-Methoxy-1,4-naphthoquinone (2348-82-5)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
QL8960000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
189162
Product name
2-Methoxy-1,4-naphthoquinone
Purity
98%
Packaging
5g
Price
$93
Updated
2024/03/01
AK Scientific
Product number
1362AQ
Product name
2-Methoxy-1,4-naphthoquinone
Packaging
5g
Price
$147
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0078225
Product name
2-METHOXY-1,4-NAPHTHOQUINONE
Purity
95.00%
Packaging
5G
Price
$857.17
Updated
2021/12/16
Arctom
Product number
CFN95269
Product name
2-Methoxy-1,4-naphthoquinone
Purity
≥98%
Packaging
20mg
Price
$70
Updated
2021/12/16
AHH
Product number
MT-16989
Product name
2-Methoxy-1,4-naphthoquinone
Purity
98%
Packaging
100g
Price
$345
Updated
2021/12/16
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2-METHOXY-1,4-NAPHTHOQUINONE Chemical Properties,Usage,Production

Uses

2-Methoxy-1,4-naphthoquinone was used in the preparation of 2-(4-X-phenylene)amine-1,4-naphthoquinones (X= ferrocenyl, OMe, Me, I, Cl and NO2).

Definition

ChEBI: A naphthoquinone that is naphthalene-1,4-dione substituted by a methoxy group at position 2. It has been isolated from the roots of Rubia yunnanensis.

General Description

2-Methoxy-1,4-naphthoquinone is a potential candidate for Helicobacter pylori infection related disease therapy. It is isolated from the leaves of Impatiens glandulifera.

2-METHOXY-1,4-NAPHTHOQUINONE Preparation Products And Raw materials

Raw materials

Preparation Products

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2-METHOXY-1,4-NAPHTHOQUINONE Suppliers

Target molecule Corp.
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857-239-0968
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2348-82-5, 2-METHOXY-1,4-NAPHTHOQUINONERelated Search:


  • 1,4-Naphthoquinone, 2-methoxy-
  • 2-methoxy-1,4-naphthalenedione
  • 2-methoxy-4-naphthalenedione
  • 2-methoxy-4-naphthoquinone
  • 2-Methoxynaphthoquinone
  • 2-Methoxy-p-naphthoquinone
  • 2-METHOXY-1,4-NAPHTHOQUINONE
  • 2-METHOXY-1,4-NAPTHOQUINONE, 98+% SEE S 45484-2
  • 2-Methoxy-1,4-naphtoquinone
  • Lawsone methyl ether
  • 2-methoxynaphthalene-1,4-dione
  • 2-Methoxy-1,4-naphthoquinone 98%
  • 1,4-Naphthalenedione, 2-methoxy-
  • balsamina,Bacterial,Lawsone methyl ether,antifungal,calycina,Impatiens,antibacterial,Inhibitor,inhibit,Swertia,Fungal
  • 2348-82-5
  • C11 to C12
  • Carbonyl Compounds
  • Building Blocks
  • Ketones
  • Organic Building Blocks
  • Inhibitors
  • C11 to C12
  • Carbonyl Compounds
  • Ketones
  • Building Blocks
  • C11 to C12
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks